Saprochaete clavata infections in patients undergoing treatment for haematological malignancies: A report of a monocentric outbreak and review of the literature

伏立康唑 氟康唑 内科学 棘白菌素 米卡芬金 恶性肿瘤 医学 医学微生物学 生物 抗真菌 免疫学 皮肤病科
作者
Marta Stanzani,Monica Cricca,Claudia Sassi,Emanuele Sutto,Gabriella De Cicco,Francesca Bonifazi,Clara Bertuzzi,Francesco Bacci,Stefania Paolini,Michèle Cavo,Russell E. Lewis
出处
期刊:Mycoses [Wiley]
卷期号:62 (12): 1100-1107 被引量:20
标识
DOI:10.1111/myc.12978
摘要

Summary Saprochaete clavata is a rare cause of fungaemia with deep organ involvement in patients with haematological malignancies with reported mortality rates of 60%‐80%. We describe four cases of S clavata infection in a haematology unit over several months that were treated with voriconazole‐based regimens. We also review the literature on factors that could contribute to earlier recognition and effective treatment of S clavata . We included all cases of culture‐positive S clavata from sterile sites with associated signs of infection in patients undergoing treatment for a haematological malignancy. Isolates were identified by MALDI ‐ TOF MS , and spectrum profiles were used to prepare clustering analysis of isolates. Susceptibility testing was performed using a commercial microtitre methods. Saprochaete clavata was isolated from the bloodstream in three cases and bronchial alveolar lavage ( BAL ) fluid in one case. Clustering analysis suggested strains of S clavata were clonal without evidence of divergence although a common source was not identified. Susceptibility testing yielded elevated MIC s to fluconazole (8 mg/L) and echinocandins (>1‐8 mg/L). All patients were treated with voriconazole‐based regimens resulting in survival of 3/4 patients, who continued chemotherapy for their underlying malignancy without evidence of relapse. Saprochaete clavata is a rare but aggressive cause of breakthrough yeast infection in patients undergoing treatment for haematological malignancies, particularly patients with a prior history of echinocandin treatment. Timely initiation of appropriate treatment, aided by more rapid identification in microbiology laboratory, can reduce the risk of deep organ dissemination and patient death.
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